# K071335: Medpor Attractor Implant

- Pathway: 510(k) (Traditional)
- Applicant: Porex Surgical, Inc.
- Decided: Aug 8, 2007 after 89 days
- Product code: HPZ (Implant, Eye Sphere)
- Device class: 2
- Regulation: 21 CFR 886.3320
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) MEDPOR ATTRACTOR Magnetic Coupling System: named in the summary without a submission number
- (no number) MEDPOR Surgical Implant Material; Preformed Cranial & Facial Implants: named in the summary without a submission number

## Indications for use
The MEDPOR ATTRACTOR Implant is intended for patients who require replacement of volume in an enucleated or eviscerated orbit and who wish to gain improved prosthetic eye motility by coupling the MEDPOR ATTRACTOR Implant to the prosthetic eye.

Source page: https://510kreport.com/device/K071335
Methodology: https://510kreport.com/methodology